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Jyotsna Sudi

Showing results (1-10 of 14) with videos related to

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Genetics|May 22, 2008
Coincidence of P-insertion sites and breakpoints of deletions induced by activating P elements in DrosophilaJyotsna Sudi, Sen Zhang, Gino Intrieri, et al.
American Journal of Medical Genetics. Part A|March 19, 2011
Corpus callosum agenesis, severe mental retardation, epilepsy, and dyskinetic quadriparesis due to a novel mutation in the homeodomain of ARXValerio Conti, Carla Marini, Simone Gana, et al.
Autism Research : Official Journal of the International Society for Autism Research|December 24, 2009
Copy number and sequence variants implicate APBA2 as an autism candidate geneTimothy D Babatz, Ravinesh A Kumar, Jyotsna Sudi, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Duplication 16p11.2 in a child with infantile seizure disorderJirair K Bedoyan, Ravinesh A Kumar, Jyotsna Sudi, et al.
American Journal of Respiratory and Critical Care Medicine|October 17, 2015
Genome-Wide Methylation Study Identifies an IL-13-induced Epigenetic Signature in Asthmatic AirwaysJessie Nicodemus-Johnson, Katherine A Naughton, Jyotsna Sudi, et al.
Journal of Medical Genetics|June 24, 2009
A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autismRavinesh A Kumar, Jyotsna Sudi, Timothy D Babatz, et al.
Brain : a Journal of Neurology|May 15, 2009
Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous femalesEric Marsh, Carl Fulp, Ernest Gomez, et al.
European Journal of Pediatrics|October 20, 2009
Microcephaly, sensorineural deafness and Currarino triad with duplication-deletion of distal 7qPiero Pavone, Martino Ruggieri, Ilaria Lombardo, et al.
Human Molecular Genetics|December 25, 2007
Recurrent 16p11.2 microdeletions in autismRavinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, et al.
The Journal of Allergy and Clinical Immunology|March 29, 2013
Maternal asthma and microRNA regulation of soluble HLA-G in the airwayJessie Nicodemus-Johnson, Bharathi Laxman, Randi K Stern, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Genetics|May 22, 2008
Coincidence of P-insertion sites and breakpoints of deletions induced by activating P elements in DrosophilaJyotsna Sudi, Sen Zhang, Gino Intrieri, et al.
American Journal of Medical Genetics. Part A|March 19, 2011
Corpus callosum agenesis, severe mental retardation, epilepsy, and dyskinetic quadriparesis due to a novel mutation in the homeodomain of ARXValerio Conti, Carla Marini, Simone Gana, et al.
Autism Research : Official Journal of the International Society for Autism Research|December 24, 2009
Copy number and sequence variants implicate APBA2 as an autism candidate geneTimothy D Babatz, Ravinesh A Kumar, Jyotsna Sudi, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Duplication 16p11.2 in a child with infantile seizure disorderJirair K Bedoyan, Ravinesh A Kumar, Jyotsna Sudi, et al.
American Journal of Respiratory and Critical Care Medicine|October 17, 2015
Genome-Wide Methylation Study Identifies an IL-13-induced Epigenetic Signature in Asthmatic AirwaysJessie Nicodemus-Johnson, Katherine A Naughton, Jyotsna Sudi, et al.
Journal of Medical Genetics|June 24, 2009
A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autismRavinesh A Kumar, Jyotsna Sudi, Timothy D Babatz, et al.
Brain : a Journal of Neurology|May 15, 2009
Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous femalesEric Marsh, Carl Fulp, Ernest Gomez, et al.
European Journal of Pediatrics|October 20, 2009
Microcephaly, sensorineural deafness and Currarino triad with duplication-deletion of distal 7qPiero Pavone, Martino Ruggieri, Ilaria Lombardo, et al.
Human Molecular Genetics|December 25, 2007
Recurrent 16p11.2 microdeletions in autismRavinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, et al.
The Journal of Allergy and Clinical Immunology|March 29, 2013
Maternal asthma and microRNA regulation of soluble HLA-G in the airwayJessie Nicodemus-Johnson, Bharathi Laxman, Randi K Stern, et al.
Pageof 2